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Manufacturing Manager

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Onsite

Manufacturing Manager

5th HQ

Manufacturing Manager

Skills

Process ImprovementCompliance

1 year ago

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Important information


Contract type:

Permanent

Salary:

$62,400 / year

Location:

Miramar, FL, USA

Work mode:

Onsite

Published on:

15 October 2026

What they need


We are seeking an experienced Manufacturing Manager to lead and oversee day-to-day operations within our nutraceutical/pharmaceutical production facility. The ideal candidate will bring proven leadership in cGMP-compliant environments and possess a strong background in managing production teams, ensuring regulatory compliance, and driving continuous improvement in quality, efficiency, and safety.

Location: Miramar, FL
Compensation: $30 per hour
Schedule:

  • Standard Office Hours: 8:30 AM – 5:00 PM
  • Flex Shift (as needed): 10:00 AM – 7:00 PM

Preferred Background:

  • Prior experience in nutraceutical or pharmaceutical manufacturing is highly preferred.
  • Strong understanding of OSHA, FDA, and cGMP regulations.
  • Familiarity with world-class manufacturing methods and statistical process control.

Minimum Qualifications:

  • Bachelor’s Degree (B.A. or B.S.) required.
  • 4–5 years of manufacturing supervisory experience in a cGMP-regulated facility.
  • Strong leadership and team-building skills.
  • Excellent verbal and written communication skills.
  • Proven ability to analyze production performance and implement improvements.
  • Working knowledge of manufacturing documentation, SOPs, and quality control practices.

Key Responsibilities:

  • Lead and manage the manufacturing department, ensuring smooth daily operations and alignment with company goals.
  • Report directly to the COO while collaborating cross-functionally with QC, Sales, Operations, CEO, and CFO.
  • Establish and enforce production procedures to maintain high-quality standards, safety, and operational efficiency.
  • Ensure compliance with cGMP, SOPs, and company quality systems.
  • Oversee production scheduling, staffing, and shift planning—including managing overtime and additional shifts as necessary.
  • Monitor production runs to ensure they stay on schedule and troubleshoot any delays or issues.
  • Continuously evaluate and improve efficiency, machine utilization, and resource allocation.
  • Oversee batch record documentation, ensuring accuracy, completeness, and compliance with regulations.
  • Analyze finished goods (capsules and tablets) to ensure they meet specifications for potency, weight, and quality.
  • Provide regular training to team members on GMP practices, SOP compliance, and safety procedures.
  • Promote a clean, organized, and accident-free work environment by enforcing all safety protocols.
  • Identify areas for cost savings and implement strategies for lean manufacturing and continuous improvement.

Preferred Skills & Traits:

  • Bilingual (English/Spanish) is a plus.
  • Proficient in Microsoft Office and experience with ERP systems.
  • Knowledge of Lean Manufacturing, Six Sigma, or similar process improvement methodologies is beneficial.

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